Safety and Immunogenicity of Different Formulations of an Adjuvanted, Trivalent Subunit Influenza Vaccine in Elderly Subjects 65 Years of Age and Above

Influenza Clinical Trial

Official title:

A Phase 1, Randomized, Observer Blind, Antigen and Adjuvant Dosage-Finding Study to Evaluate the Safety and Immunogenicity of an Adjuvanted, Trivalent Subunit Influenza Vaccine in Elderly Subjects ≥65 Years of Age

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02126761
• Other study ID #: V133_01EXP
• Secondary ID: 2013-005344-29
• Status: Completed
• Phase: Phase 1
• First received: April 28, 2014
• Last updated: July 28, 2016
• Start date: June 2014
• Est. completion date: November 2015

Study information

• Verified date: December 2015
• Source: Seqirus
• Contact: n/a
• Is FDA regulated: No
• Health authority: Germany: Paul-Ehrlich-Institut
• Study type: Interventional

Clinical Trial Summary

In this study, the safety and immunogenicity of the current formulation of aTIV will be compared to aTIV-modified formulations in which the dosage of the MF59 adjuvant will be doubled or tripled and/or the dosage of the 3 influenza virus strains will be doubled, in independently-living elderly subjects ≥ 65 years of age.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 196
• Est. completion date: November 2015
• Est. primary completion date: November 2015
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 65 Years and older

Eligibility

Inclusion Criteria:

1. Male and female subjects =65 years of age on the day of screening who are healthy or have chronic illnesses that are stable and well controlled.

2. Subjects assessed as mentally competent, who have given informed consent after the nature of the study has been explained according to local requirements

3. In good health as determined by:

1. Ability to live independently

2. Medical history

3. Physical examination

4. Clinical judgment of the Investigator

4. Able to understand and comply with all study procedures and visits, and are able to complete an eDiary

5. Individuals who have access to a working telephone and are able to receive periodic telephone calls

Exclusion Criteria:

1. Individuals who have received any type of influenza vaccine (licensed or experimental) within the past 6 months

2. Individuals who have received any other licensed vaccines within 30 days (for inactivated vaccines) or 42 days (for live vaccines) prior to enrollment in this study

3. Individuals who have cancer except for:

1. Benign localized skin cancer

2. Localized prostate cancer that has been clinically stable for = 2 years without treatment

3. Cancer in remission for = 10 years (from end of cancer treatment)

4. Individuals with autoimmune disease (including rheumatoid arthritis)

5. Individuals with diabetes mellitus, type I

6. Individuals with a body mass index (BMI) =18 or =35.

7. Asthma that is greater than mild in severity and / or has exacerbations more than 2 days per week

8. Congestive heart failure with symptoms as severe as or more severe than dyspnea with short walks or climbing a single flight of stairs (for example, greater than New York Heart Association class 2)

9. History of progressive or severe neurologic disorders including but not limited to multiple sclerosis, Parkinson's disease, Guillain-Barré syndrome, amyotrophic lateral sclerosis, Creutzfeldt-Jakob disease, epilepsy disorders requiring medication for control, encephalitis, Alzheimer's and CVA

10. Individuals who are hypersensitive to ovalbumin, chicken protein, chicken feathers, influenza viral protein, kanamycin and neomycin sulfate or any other component of the vaccines in study

11. Individuals who have a history of neurological symptoms or signs, or anaphylactic shock following administration of any vaccine

12. Individuals who have a known or suspected (or have a high risk of developing) impairment/alteration of immune function resulting from, for example,

a. Receipt of immunosuppressive therapy (defined as follows) within the past 60 days and/or anticipated to receive immunosuppressive therapy at any point within 21 days of Visit 1.

i. Cancer chemotherapy/radiotherapy ii. Systemic corticosteroids ( i.e., 15 mg or greater per day of prednisone or equivalent) iii. Chronic use of inhaled/intranasal high potency corticosteroids (budesonide 800 µg per day or fluticasone 750 µg per day) b. Receipt of immunostimulants c. Receipt of parenteral immunoglobulin preparation, blood products and/or plasma derivate within the past 3 months and for the full length of the study d. Suspected or known HIV infection or HIV-related disease

13. Individuals who have a known or suspected history of drug or alcohol abuse

14. Individuals who, within the past 12 months, have had laboratory confirmed influenza disease

15. Individuals who, within the past 30 days have received any investigational agent.

16. Individuals who plan to receive another vaccine within 30 days of receipt of the study vaccination.

17. Individuals who, within the past 14 days, have experienced:

1. Any acute disease including any worsening of underlying respiratory diseases such as asthma or COPD

2. Infections requiring systemic antibiotic or antiviral therapy (chronic antibiotic therapy for urinary tract prophylaxis is acceptable)

18. Individuals who are taking part in another clinical study

19. Individuals who are research staff directly involved with the clinical study or family members or household members of research staff. Research staff includes an individual with direct or indirect contact with study subjects, or study site personnel who have access to any study documents containing subject information. This would include receptionists, persons scheduling appointments or making screening calls, regulatory specialists, laboratory technicians, etc.

20. Individuals with behavioral or cognitive impairment or a psychiatric condition that, in the opinion of the investigator, may interfere with the subject's ability to participate in the study.

21. Vulnerable subjects, e.g. subjects kept in detention, soldiers, employees of the sponsor or a clinical research organization involved in this study

22. Individuals who have any condition which, in the opinion of the investigator, might interfere with the evaluation of the study objectives.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Factorial Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention

Related Conditions & MeSH terms

• Influenza
• Influenza, Human

Intervention

Biological:
• Adjuvanted, trivalent subunit influenza vaccine
Group 1 and group 5 are active comparators; group 5 includes placebo comparator as a second injection in contralateral deltoid
• Adjuvant level modified adjuvanted, trivalent subunit influenza vaccine
Group 2 and group 6 are experimental; group 2 has double dosage of MF59 in a single injection; group 6 has triple dosage of MF59 and includes placebo comparator in contralateral deltoid
• Antigen level modified adjuvanted, trivalent subunit influenza vaccine
Group 3 is experimental with double the usual antigen dosage
• Antigen and adjuvant level modified adjuvanted, trivalent subunit influenza vaccine
Group 4 and 7 are experimental; group 4 has one injection with double the antigen and adjuvant; group 7 has two injections with double the antigen and adjuvant

Locations

Country	Name	City	State
Germany	PAREXEL Early Phase Clinical Unit	Berlin

Sponsors (2)

Lead Sponsor	Collaborator
Seqirus	Novartis Vaccines

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Reactogenicity up to 7 days after vaccination	Safety of aTIV or aTIV-modified formulations	Days 1-7 post-vaccination	Yes
Primary	Unsolicited AEs within 28 days after vaccination		Days 1-28 post-vaccination	Yes
Primary	SAEs, non-scheduled physician visits, unsolicited medically attended AEs, unsolicited AEs leading to study withdrawal, NOCDs, and AESIs from study start to study completion.		Days 1-366 post-vaccination	Yes
Primary	Seroconversion/significant increase in antibody HI titers; =4-fold rise in MN titer 21 days post-vaccination.	Antibody responses to all three influenza virus vaccine strains, 21days after a dose or doses of aTIV or aTIV-modified formulations, as measured by hemagglutination inhibition (HI) assay and microneutralization (MN) assay.	Day 22 post-vaccination	No
Primary	HI and MN GMT and GMR at baseline and 21 days post-vaccination.		Day 1; Day 22 post-vaccination	No
Secondary	Seroconversion/significant increase in antibody HI titers; =4-fold rise in MN titer, 7 days and 6 months post-vaccination.		Day 8 and 181 post-vaccination	No
Secondary	HI and MN (GMT) 7 days and 6 months post-vaccination.	To compare HI and MN responses to a aTIV or aTIV-modified formulations, at 7 days and 6 months post-vaccination.	Day 8 and 181 post-vaccination	No
Secondary	HI and MN (GMR) 7 days, 21 days, and 6 months post-vaccination.		Day 1, 8, 22, and 181 post-vaccination	No
Secondary	Percentage of subjects with HI titers =1:40, =1:110, =1:160, and =1:330 7 days, 21 days, and 6 months post-vaccination.	To compare antibody responses in subjects receiving aTIV-modified formulations in a single intramuscular injection (in one deltoid) to two intramuscular injections (one in each deltoid) at 7 days, 21 days, and 6 months post-vaccination.	Day 8, 22, and 181 post-vaccination	No